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Metadata
ID	DOID:0110080
Name	Leber congenital amaurosis 12
Definition	A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/17186464
Xrefs	ICD10CM:H35.5 MESH:C565697 MIM:610612
Synonyms	LCA12 [EXACT]
Parent Relationships	is_a Leber congenital amaurosis is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance disease has basis in some Abnormality of prenatal development or birth